R E S E A R C H A R T I C L E
Open Access
Association of 25-hydroxyvitamin D deficiency
with NT-pro BNP levels in patients with acute
myocardial infarction: a cross-sectional analysis
James B Wetmore
1,2,3*, Rajyalakshmi Gadi
1, John H Lee
4, James H O
’
Keefe
4, Paul S Chan
4, Fengming Tang
4and
John A Spertus
4Abstract
Background:Nutritional vitamin D deficiency is an emerging risk factor for acute myocardial infarction (AMI) and heart failure. The association of 25-hydroxyvitamin D levels with N-terminal pro B-type natriuretic peptide (NT-proBNP), a robust prognostic marker for post-AMI mortality and heart failure, is unknown and could illuminate a potential pathway for adverse outcomes among post-AMI patients with 25-hydroxyvitamin D deficiency.
Methods:In a cross-sectional analysis, we studied 238 AMI patients from 21 U.S. centers to test the association of nutritional vitamin D (25-hydroxyvitamin D [25(OH)D]) deficiency with NT-proBNP levels. Levels of 25(OH)D levels were categorized as normal (≥30 ng/mL), insufficient (>20 - <30 ng/mL), deficient (>10 -≤20 ng/mL), or severely deficient (≤10 ng/mL).
Results:Low 25(OH)D levels were found in 95.7% of AMI patients. No significant trends for higher mean baseline log NT-proBNP levels in severely deficient (6.9 ± 1.3 pg/mL), deficient (6.9 ± 1.2 pg/mL), and insufficient (6.9 ± 0.9 pg/ml) groups were observed as compared with patients having normal (6.1 ± 1.7 pg/mL) levels,P= 0.17. Findings were similar in the subset of patients who had follow-up NT-proBNP levels drawn at one month. In multivariate regression modeling, after adjusting for multiple covariates, 25(OH)D was not associated with NT-proBNP.
Conclusions:Potential associations between nutritional vitamin D deficiency and prognosis in the setting of AMI are unlikely to be mediated through NT-proBNP pathways. Future studies should examine other mechanisms, such as inflammation and vascular calcification, by which 25(OH)D deficiency could mediate adverse outcomes post-AMI.
Keywords:Vitamin D, N-terminal proBNP, Acute myocardial infarction
Background
Deficiency in nutritional vitamin D [25-hydroxyvitamin D, or 25(OH)D] is highly prevalent, occurring in approximately 30%-50% of the general population [1,2] and in an even greater percentage of hospitalized patients [3]. In several studies, 25(OH)D deficiency has been independently associated with both incident acute myocardial infarction (AMI) and heart failure (HF) [4,5], suggesting that 25(OH)D plays an important role in car-diac function. In support of this hypothesis, several in vitro studies have shown that calcitriol (1,25(OH)2D3),
an active form of vitamin D, regulates intracellular cal-cium metabolism and myocardial contractility through specific vitamin D receptors on cardiac myocytes [5-8]. Consequently, 25(OH)D deficiency has been associated with aberrant cardiac contractility, cardiomegaly, and increased ventricular mass due to myocardial collagen deposition [6,7], independent of its known effects on blood pressure [6]. In studies of experimental animals, activation of nuclear vitamin D receptors by 1,25(OH)
2D3 suppresses the expression and secretion of atrial
natriuretic peptide (ANP) and brain natriuretic peptide (BNP) in cardiac myocytes [9-13], while in clinical stu-dies of nondialysis chronic kidney disease patients, indi-viduals treated with 1,25(OH)2D3 for 12 weeks were
observed to have improved left ventricular diastolic
* Correspondence: jwetmore@kumc.edu
1
Division of Nephrology and Hypertension, University of Kansas Medical Center, Kansas City, KS, USA
Full list of author information is available at the end of the article
function as compared with placebo [14]. Collectively, these findings suggest that low circulating levels of 25 (OH)D could contribute to, or potentiate, the develop-ment of left ventricular dysfunction and HF after AMI.
In recent years, N-terminal pro B-type natriuretic pep-tide (NT-proBNP), a prohormone of BNP released from cardiac ventricles, has been associated with the severity of left ventricular dilatation and dysfunction after AMI [15,16]. In addition, NT-proBNP is a sensitive and robust prognostic biomarker of mortality in AMI [15,17-19], HF [20,21] and chronic hemodialysis patients [22,23]. Moreover, NT-proBNP levels have direct clinical implications, as they are used to guide therapeutic inter-ventions in HF patients and lead to improved outcomes as compared with routine clinical treatment [24].
While both 25(OH)D and NT-proBNP are known to be associated with LV dysfunction after AMI, it is not known whether there is a correlation between levels of 25(OH)D and NT-proBNP in this setting. In clinical stu-dies, inverse associations between 25(OH)D levels and NT-proANP in HF [5] and between 25(OH)D and BNP in dialysis patients have been reported [25,26]. However, these studies had small sample sizes and were not based on patients living in the U.S., where better nutrition and fortification of milk is common [27]. Given the adverse health implications of 25(OH)D deficiency and the lack of studies in AMI patients (a particularly high-risk group), we sought to examine the association of 25(OH) D deficiency with NT-proBNP levels in a multicenter cohort of AMI patients. Discovery of an association between circulating levels of 25(OH)D and NT-proBNP would not only suggest a potential pathway for adverse outcomes among post-AMI patients with 25(OH)D defi-ciency, but could also identify a potentially novel
thera-peutic target (i.e., nutritional vitamin D
supplementation) to reduce NT-proBNP levels, in the hopes of improving prognosis after AMI.
Methods
Study participants
The present study is a cross-sectional analysis of a long-itudinal cohort study. Participants were drawn from the TRIUMPH (Translational Research Investigating Under-lying disparities in recovery from acute Myocardial infarction: Patients’Health status) study, a prospective multicenter cohort study of AMI patients across 21 U.S. centers [28]. Patients were eligible for TRIUMPH if they were ≥ 18 years of age and had a diagnosis of AMI. AMI was diagnosed by the presence of either a CK-MB elevation greater than twice normal or a troponin-I ele-vation of >0.1 mg/ml within 24 h of arrival to the hospi-tal, accompanied by a clinical presentation suggestive of an AMI (e.g., prolonged ischemic signs or chest pain symptoms, at least one EKG with ST-wave elevation or
ST-wave depression in 2 or more consecutive leads, and no alternative explanation for the presence of elevated serum cardiac markers). Patients were excluded if they transferred to the participating hospital from another facility greater than 24 h after their original AMI pre-sentation, if they refused or could not provide informed consent, or if they were receiving hospice care. For this study, we included the last 250 TRIUMPH patients, in each of whom 25(OH)D levels were assessed in addition to the standard data collected [29]. TRIUMPH complied with the principles of the Declarations of Helsinki and was approved by the institutional review board at the coordinating center, Mid America Heart Institute at St. Luke’s Hospital (Kansas City, MO). Written informed consent was obtained from all participants.
Data collection
During index hospitalization, trained data collectors per-formed a patient interview and detailed chart abstraction within 24-72 h of admission. Patient data at AMI pre-sentation, including demographic features, socioeco-nomic status, comorbidities, severity of AMI (ST elevation present or not), Killip class, Rose dyspnea index, vital signs, and laboratory values were abstracted. The Rose dyspnea score is a validated self-reported question in AMI patients that is scored from 0-4, with higher scores indicating worse dyspnea [30]. Regional and seasonal data were collected, given their association with 25(OH)D levels [31,32]. Patients were classified by their residing states in to 5 U.S. geographic regions, namely northeast (NE), southeast (SE), southwest (SW), midwest (MW) and west (W). Months of April-June, July-August and September-December were classified as summer, fall, and early winter seasons, respectively.
Left ventricular systolic function (LVSF) was classified as normal, mild, moderate or severe as assessed by echocardiography, angiography or nuclear imaging and documented in the hospital record. Finally, reperfusion therapy (percutaneous intervention [PCI] and/or coron-ary artery bypass surgery [CABG]) and other acute therapies, as well as medications prescribed at hospital discharge, were recorded. Blood samples from all con-senting patients were sent to a core laboratory (Clinical Reference Laboratories, Lenexa, KS, USA) for NT-proBNP measurement (Roche Diagnostics, Indianapolis, IN, USA) and 25(OH)D assays, as described below.
Laboratory measurements
metabolites from serum or plasma with acetonitrile along with a 25(OH)D-specific antibody and tracer, and phase separation with a second antibody-precipitating complex. The total (intra-and inter-assay) precision of the assay has a coefficient of variation (CV) of 9.4% and 11% for control values of 8.6 ng/mL and 49.0 ng/ml, respectively.
For measurement of circulating NT-proBNP levels, the Roche electro-chemiluminescence immunoassay for the in vitro quantization was used (ECLIA Roche diagnos-tics, Mannheim, Germany). The precision of this assay was represented by a CV of 3.2% and 2.3% for control values of 175 pg/mL and 4962 pg/mL, respectively. Blood samples for NT-proBNP were drawn immediately prior to hospital discharge. The mean time of the NT-proBNP blood draw was 3.5 ± 4 days after enrollment. Glomerular filtration rate (eGFR) was estimated using the four variable Modification of Diet in Renal Disease (MDRD) study equation [34].
Statistical analysis
Participants were classified into clinically-relevant cate-gories on the basis of 25(OH)D levels. Patients with levels≥30 ng/mL were classified as normal, while levels >20 ng/mL and <30 ng/ml were considered insufficient, levels of >10 to≤20 ng/ml were deficient, and levels≤10 ng/mL were severely deficient. Median NT-proBNP levels were compared using the non-parametric Kruskal-Wallis test, due to the positively-skewed distribution of proBNP. Log proBNP and quartiles of NT-proBNP were compared across the four 25(OH)D strata using ANOVA and chi-square tests, respectively, both at baseline and, in a complementary analysis, in the sub-group of patients who had 1-month levels of NT-proBNP levels drawn. To confirm previously-reported relationships, log NT-proBNP and category of LVSF was analyzed with the linear trend test. Spearman rank cor-relation was obtained between NT-proBNP and 25(OH) D levels. Multivariable linear regression analysis to determine the association of 25(OH)D levels with log NT-proBNP was performed, adjusting for relevant cov-ariates and confounders. The presence of a potential interaction between NT-proBNP levels and type of AMI (i.e., ST-elevation versus non-ST-elevation) was formally tested using the likelihood ratio test. A P-value of <0.05 was considered statistically significant. All analyses were conducted using SAS v9.1 software (Cary, NC, U.S.).
Results
Of the 238 enrolled patients on whom sufficient data was available, the median 25(OH)D concentration was 16 ng/mL (interquartile range [IQR], 12-21 ng/mL). As noted previously [29], classification of 25(OH)D levels into more clinically-interpretable ranges showed 40
(16.8%) to be severely deficient, 138 (57.9%) to be defi-cient, and 50 (21.0%) to be insufficient. Only 4.2% of participants in the study had normal 25(OH)D levels, with none of the African-American participants having normal levels.
Characteristics of participants across 25(OH)D groups are shown in Table 1. No statistically-significant differ-ences by age or gender were noted across 25(OH)D groups. Deficiency in 25(OH)D was associated with non-Caucasian (i.e., African-American) race, lower socioeconomic status indicators, a history of recent smoking, and lower levels of physical activity. No differ-ence in those with or without 25(OH)D deficiency were observed for diabetes, hypertension, chronic kidney dis-ease, chronic HF, left ventricular hypertrophy on admis-sion electrocardiogram, Kullip class, Rose dyspnea score, or the type of AMI (STEMI vs. NSTEMI). During the study period, no statistically-significant regional varia-tions were observed in patients’ enrollment across 25 (OH)D groups, although there was a trend towards sea-sonal variation in 25(OH)D levels (P = 0.064), with the winter months being associated with the lowest levels. Estimated glomerular filtration rates did not differ. In terms of laboratory values, lower serum calcium and higher parathyroid hormone (PTH) levels were signifi-cantly associated with 25(OH)D deficiency (P= 0.03 and P= 0.004, respectively), as would be expected. Likewise, the use of omega-3 supplements was significantly greater higher in patients with normal 25(OH)D levels compared to those who had insufficient, deficient, or severely-deficient levels (P= 0.002).
Continuous data shown as mean ± 1 standard devia-tion. 25(OH)D, 25-hydroxyvitamin D; BMI, body mass index; MI, myocardial infarction; CKD, chronic kidney disease; LVH, left ventricular hypertrophy; ECG, elec-trocardiogram; MI, myocardial infarction; STEMI, ST-segment elevation myocardial infarction; LV, left ven-tricular; HDL, high density lipoprotein; LDL, low den-sity lipoprotein; PTH, parathyroid hormone; hs-CRP, high sensitivity C-reactive protein; eGFR, estimated glomerular filtration rate; ACEI, angiotensin convert-ing enzyme inhibitor; ARB, angiotensin receptor blocker.
Table 1 Baseline characteristics of study participants, by 25(OH)D group
25(OH)D group, ng/mL
0-10 >10-≤20 >20-<30 ≥30
Characteristic (n= 40) (n= 138) (n= 50) (n= 10) P-value
Demographics
Age (yr) 55.0 ± 11.2 57.8 ± 11.8 58.8 ± 10.2 62.4 ± 11.3 0.21
Male,n(%) 26(65.0) 104(75.4) 38 (76.0) 8 (80.0) 0.57
Caucasian,n(%) 23 (57.5) 103 (74.6) 41 (82.0) 10 (100.0) 0.012
BMI (kg/m2) 32.1 ± 5.6 30.9 ± 6.9 29.5 ± 5.6 26.5 ± 4.6 0.066
Socio-economic status
Low social support,n(%) 11 (27.5) 20 (14.9) 3 (6.0) 0 (0) 0.023 No health insurance,n(%) 14 (35.0) 28 (20.9) 5 (10.4) 1 (10.0) 0.036 Lifestyle
Smoked within 1 month,n(%) 24 (60.0) 49 (35.5) 15 (30.0) 0(0) <0.001
Leisure time activity,n(%) 0.047
Mainly sedentary 20 (50.0) 56 (40.9) 19 (38.0) 1 (10.0)
Mild exercise 13 (32.5) 49 (35.8) 11 (22.0) 3 (30.0)
Moderate exercise 6 (15.0) 27 (19.7) 17 (34.0) 4 (40.0)
Strenuous exercise 1 (2.5) 5 (3.6) 3 (6.0) 2 (20.0)
Geographical region,n(%) 0.79
Midwest 18 (56.3) 53 (45.3) 15 (34.1) 5 (62.5)
Northeast 3 (9.4) 15 (12.8) 5 (11.4) 0 (0)
Southeast 5 (15.6) 23 (19.7) 9 (20.5) 1 (12.5)
Southwest 4 (12.5) 22 (18.8) 12 (27.3) 2 (25.0)
West 2 (6.3) 4 (3.4) 3 (6.8) 0 (0)
Season,n(%) 0.064
Apr-Jun 1 (2.5) 1 (0.7) 0 (0) 0 (0)
Jul-Sep 10 (25.0) 56 (40.6) 24 (48.0) 7 (70.0)
Oct-Dec 29 (72.5) 81 (58.7) 26 (52.0) 3 (30.0)
Comorbidities,n(%)
Diabetes 13 (32.5) 41 (29.7) 8 (16.0) 2 (20.0) 0.21
Hypertension 26 (65.0) 89 (64.5) 33 (66.0) 6 (60.0) 0.99
Prior MI 2 (5.0) 36 (26.1) 9 (18.0) 2 (20.0) 0.019
CKD 5 (12.5) 4 (2.9) 2 (4.0) 1 (10.0) 0.06
Chronic heart failure 3 (7.5) 6 (4.3) 1 (2.0) 1 (10.0) 0.38
LVH on admission ECG,n(%) 7 (17.9) 9 (6.7) 4 (8.2) 0 (0) 0.18
Killip class on arrival,n(%) 0.35
I 36 (94.7) 128 (94.8) 43 (86.0) 9 (90.0)
II 2 (5.3) 4 (3.0) 5 (10.0) 1 (10.0)
III 0 (0) 2 (1.5) 2 (4.0) 0 (0)
IV 0 (0) 1 (0.7) 0 (0) 0 (0)
Rose dyspnea score 1.0 ± 0.9 0.9 ± 0.9 0.8 ± 0.8 0.6 ± 1.0 0.43
Final MI diagnosis,n(%) 0.36
STEMI 15 (37.5) 64 (46.4) 23 (46.0) 2 (20.0)
Non-STEMI 25 (62.5) 74 (53.6) 27 (54.0) 8 (80.0)
LV systolic function,n(%) 0.54
Normal 24 (61.5) 88 (63.8) 36 (72.0) 6 (60.0)
Mild 8 (20.5) 24 (17.4) 10 (20.0) 1 (10.0)
Moderate 4 (10.3) 16(11.6) 4 (8.0) 1 (10.0)
Severe 3 (7.7) 10 (7.2) 0 (0) 2 (20.0)
Laboratory values
Troponin I (ng/ml) 1.4 ±1.9 1.7 ± 1.8 1.6 ± 1.7 0.7 ± 1.2 0.3
The association between baseline 25(OH)D and base-line log NT-proBNP levels are shown in Figure 1 and-Table 2. No statistically-significant correlation between 25(OH)D and baseline log NT-proBNP levels was observed (rho = - 0.0025,P= 0.97; Figure 1). No signifi-cant trends for higher mean log NT-proBNP levels in severely deficient (6.9 ± 1.3 pg/mL), deficient (6.9 ± 1.2 pg/mL) and insufficient (6.9 ± 0.9 pg/mL) groups were observed as compared with patients having normal (6.1 ± 1.7 pg/ml) levels, (P = 0.17; Table 2). In a sensitivity analysis, when patients were stratified into quartiles of NT-proBNP, there was also no statistically significant
association between 25(OH)D levels and category of NT-proBNP levels (P= 0.58, Table 2).
Continuous data shown as mean ± 1 standard devia-tion. 25(OH)D, 25-hydroxyvitamin D; NT-proBNP, N terminal pro brain natriuretic peptide
Because NT-proBNP levels can vary in the setting of AMI, we analyzed the subset (n = 66) of individuals who had NT-proBNP levels drawn one month after discharge. Again, there was no association between initial 25(OH)D levels and 1-month NT-proBNP levels (P= 0.82)
[image:5.595.57.540.101.249.2]In the multivariable linear regression model (shown in Table 3), after adjustment for demographic (age, race,
Figure 1Spearman correlation between levels of 25(OH)D and NT-proBNP.
Table 1 Baseline characteristics of study participants, by 25(OH)D group(Continued)
HDL(mg/dl) 37.9 ± 10.6 38.4 ± 8.7 40.6 ± 10.7 43.1 ± 25.2 0.36
LDL (mg/dl) 92.2 ± 36.7 97.4 ± 25 90.4 ± 25.7 119.2 ± 42.8 0.032 Triglycerides(mg/dl) 153.2 ± 74 185.6 ± 145 143.6 ± 79 195.4 ± 169 0.17
Calcium (mg/dl) 8.9 ± 0.6 8.8 ± 0.6 9.0 ± 0.4 9.3 ± 0.6 0.038
Intact PTH (pg/ml) 59.8 ± 67.7 40.1 ± 28.1 32.8 ± 15.3 32.0 ± 26.5 0.004
Phosphate (mg/dl) 3.6 ± 0.7 3.5 ± 0.8 3.5 ± 0.7 3.7 ± 0.9 0.69
hs-CRP (mg/l) 5.2 ± 5.6 3.8 ± 5.3 3.8 ± 4.5 0.9 ± 0.8 0.12
eGFR, mL/min/1.73 m2 84.7 ± 28.1 88.3 ± 27.3 80.3 ± 18.9 80.1 ± 18.8 0.25
Medications
ACEI/ARB,n(%) 11 (27.5) 39 (28.3) 18 (36.0) 1 (10.0) 0.43
Diuretic,n(%) 9 (22.5) 31 (22.5) 15 (30.0) 10(10.0) 0.58
[image:5.595.55.541.426.717.2]gender), anthropometric (BMI), socioeconomic (social support, medical insurance), lifestyle (smoking status), seasonal, comorbidity (diabetes and history of prior MI), treatment (in-hospital percutaneous coronary interven-tion [PCI] or coronary artery bypass graft [CABG]), laboratory (high sensitivity C-reactive protein [hs-CRP], estimated GFR) and medication (omega-3 supplement use) factors, 25(OH)D levels were not significantly asso-ciated with log NT-proBNP levels (P = 0.12). However, NT-proBNP levels were independently and strongly associated with age, race, hs-CRP, and eGFR.
BMI, body mass index; MI, myocardial infarction; PCI, percutaneous coronary intervention; CABG, coronary artery bypass graft; hs-CRP, high sensitivity C-reactive protein; eGFR, estimated glomerular filtration rate; 25 (OH)D, 25-hydroxyvitamin D
Finally, we considered the theoretical possibility that our results might be affected by type of AMI (ST-eleva-tion versus non-ST-eleva(ST-eleva-tion), so we formally tested for
an interaction between type of AMI and NT-proBNP levels; none was found (P= 0.2)
Conclusions
[image:6.595.57.540.101.225.2]In this cross-sectional observational study, we found no evidence of an association between levels of 25(OH)D and NT-proBNP upon discharge, nor was there evidence of an association at one month in the subset of tested patients. To our knowledge, this is the first study to examine levels 25(OH)D and NT-proBNP in an AMI population. Thus, while both 25(OH)D and NT-proBNP levels are associated with cardiovascular disease and heart failure, they appear to impact prognosis through different mechanisms in the setting of AMI. However, we extend our previous findings [29] in this AMI cohort by showing that 25(OH)D levels are associated with smoking, lower degrees of physical activity, and lesser use of omega-3 supplements in bivariate analysis, con-sistent with previous reports [1,31,35]. That low social support and lack of medical insurance were associated in a graded manner across fine categories of 25(OH)D level suggest that these factors, both of which are asso-ciated with higher morbidity and mortality after MI [36-38], should be investigated in more depth in future. Additionally, although our data do not support an inde-pendent association between 25(OH)D deficiency and a biomarker of left ventricular dysfunction, namely NT-proBNP, in the setting of AMI, the high prevalence of 25(OH)D deficiency, which has been associated with incident MI [4] in prior observational studies, is an important area of future investigation. It would be criti-cal to examine, for instance, whether rectifying low nutritional vitamin D levels in post-AMI patients is associated with an improvement in long-term outcomes. Our findings extend and confirm insights provided by Pilz et al., who studied patients with established CAD referred to coronary angiography [39]. While these investigators found that 25(OH)D deficiency was signifi-cantly associated with higher New York Heart Associa-tion funcAssocia-tional HF classes in unadjusted analysis, this association was no longer significant after adjustment Table 3 Multivariable regression analysis showing
association of factors with NT-proBNP levels
Covariate bcoefficient P-value
Age, per 10-yr increment 0.27 0.0006
Caucasian race 0.365 0.04
Male sex -0.165 0.31
BMI, per 5 units kg/m2increment -0.105 0.08 Lack of social support -0.209 0.31
No health insurance 0.26 0.19
Smoked within 1 month 0.03 0.85
Season, Nov-Feb vs. Mar-Oct 0.184 0.22
History of diabetes -0.02 0.9
History of prior MI 0.262 0.12
In-hospital PCI 0.202 0.23
In-hospital CABG -0.147 0.56
hs-CRP, per 5 units mg/L increment 0.449 <0.0001 eGFR, per 5 units mL/min increment -0.04 0.008
Omega-3 supplements -0.224 0.18
[image:6.595.57.291.523.730.2]25(OH)D, per 10 ng/mL increment -0.203 0.12
Table 2 Association of 25(OH)D levels with NT-proBNP levels
25(OH)D level, ng/mL
0-10 >10-≤20 >20-<30 ≥30
Characteristic (n= 40) (n= 138) (n= 50) (n= 10) P-value
Median NT-proBNP (pg/mL) 1094.5 897.5 1065.5 757.5 0.46
Mean log NT-pro BNP 6.9 ± 1.3 6.9 ± 1.2 6.9 ± 0.9 6.1 ± 1.7 0.17
NT-pro BNP (pg/mL),n(%) 0.58
for other clinical variables. In contrast, our findings are somewhat dissimilar from prior observations in chronic hemodialysis patients, where lower 25(OH)D levels were found to be associated with significantly higher log BNP levels [25]. NT-proBNP is a more stable form of BNP and correlates well with BNP levels in HF patients [40]. Similar reports in chronic HF patients have also sug-gested an inverse, nonlinear association between 25(OH) D and NT-proANP levels [5], although a clinical trial of nutritional vitamin D supplementation failed to alter patients’NT-proBNP levels [41].
More recently, a large cohort of patients referred to coronary angiography in the LUdgwigshafen RIsk and Cardiovascular Health (LURIC) study suggested that 25 (OH)D levels remained independently associated with NT-proBNP levels in a multivariable model (b= -0.180, P<0.001) [39]. It is unknown whether the discrepancy in our findings and those of previous studies is due to unmeasured confounding in prior reports, or to the impact of acute myocardial injury (present in all partici-pants of our study) on NT-proBNP levels [42,43]. Acute effects of MI could overwhelm or mask the basal asso-ciation of 25(OH)D with NT-proBNP found in a more stable condition (such as that of the participants of the LURIC study[39]), given that NT-proBNP levels are influenced by acute ischemia [33] and can change over time [44]. We did, however, specifically examine the association of 25(OH)D levels and 1-month NT-proBNP levels in a subset of patients and found results similar to our primary analysis of baseline (hospital discharge) proBNP levels, suggesting that volatility in NT-proBNP levels in the setting of AMI may not be respon-sible for our findings.
The results of our study should be interpreted in the context of some limitations. Our sample size was small, and therefore was underpowered for some analyses. However, our study of 238 patients did have 80% power to observe an unadjusted correlation of 0.18 between 25 (OH)D and NT-proBNP levels (a level comparable to that of the LURIC study[39]). Nevertheless, we cannot of course be entirely certain of our findings, so more work in this regard must be performed. Additionally, there were very few patients (n = 10) who had normal 25(OH)D levels, and if there is a non-linear association between outcome and normal 25(OH)D levels, we may have been underpowered to detect this. It is also possi-ble that the association between the biomarkers we tested might have been stronger at a time of clinical sta-bility or, conversely, at the time of acute presentation, since our samples for both 25(OH)D and NT-proBNP were taken prior to discharge; however the prognostic importance of NT-proBNP at the time of MI has consis-tently been shown to be strong [18,19], and we
performed the 1-month analysis to increase confidence in our findings.
In conclusion, the mechanism by which nutritional vitamin D deficiency mediates outcomes in AMI patients does not appear to be through its effects on, or a relationship with, NT-proBNP. Future studies should better clarify the clinical mechanism by which 25(OH)D deficiency is associated with outcomes in AMI patients. Potential candidates might include more long-term pro-cesses such as inflammation and vascular calcification. While we did not observe an association between levels of 25(OH)D and NT-proBNP, we did find a remarkably high frequency of 25(OH)D deficiency among AMI patients, consistent with other reports of hospitalized patients [3]. Hospitalization for AMI offers clinicians an opportunity to not only identify modifiable risk factors and to optimize medications for secondary prevention, but also to address other comorbidities, such as 25(OH) D deficiency. Given that nutritional vitamin D is readily available, inexpensive, and has a good safety profile, future studies should investigate whether addressing 25 (OH)D deficiency might improve outcomes in AMI patients, regardless of the mechanism of its known asso-ciation with post-AMI risk.
Abbreviations
25 (OH)D: 25-hydroxyvitamin D; AMI: Acute myocardial infarction; ANP: Atrial natriuretic peptide; BNP: Brain natriuretic peptide; CABG: Coronary artery bypass surgery; CAD: Coronary artery disease; eGFR: Estimated glomerular filtration rate; HF: Heart failure; HTN: Hypertension; hs-CRP: High sensitivity C-reactive protein; LVDF: Left ventricular dysfunction; MDRD: Modification of Diet in Renal Disease; NT-proBNP: N-terminal pro B-type natriuretic peptide; PCI: Percutaneous intervention; PTH: Parathyroid hormone levels; TRIUMPH: Translational Research Investigating Underlying disparities in recovery from acute Myocardial infarction: Patients’Health status; VSMC: Vascular smooth muscle cell.
Acknowledgements
TRIUMPH was supported by the NHLBI Specialized Center of Clinically Oriented Research in Cardiac Dysfunction and Disease (grant no. P50 HL077113) and Cardiovascular Outcomes, Inc, Kansas City, Missouri. Dr. Gadi was supported by a Genzyme, Inc, research fellowship award. The authors thank Connie Wang, MD, for technical assistance in the preparation of the manuscript.
Author details
1Division of Nephrology and Hypertension, University of Kansas Medical
Center, Kansas City, KS, USA.2University of Kansas Medical Center, Kidney
Institute, Kansas City, KS, USA.3University of Kansas Medical Center, MS 3002,
3901 Rainbow Blvd, Kansas City, KS 66160, USA.4Department of
Cardiovascular Outcomes Research, Saint Luke’s Mid America Heart Institute, Kansas City, MO, USA.
Authors’contributions
design, coordination, and analytical plan of the study and reviewed and edited the manuscript. All authors read and approved the final manuscript.
Competing interests
The authors declare that they have no competing interests.
Received: 28 October 2011 Accepted: 15 December 2011 Published: 15 December 2011
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doi:10.1186/1756-0500-4-542
Cite this article as:Wetmoreet al.:Association of 25-hydroxyvitamin D deficiency with NT-pro BNP levels in patients with acute myocardial infarction: a cross-sectional analysis.BMC Research Notes20114:542.
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